Comparision of 2 drugs (bupivacaine and levobupivacaine) in spinal anaesthesia for planned caesarean delivery.

Phase 4

• Conditions: Health Condition 1: O82- Encounter for cesarean delivery without indicationHealth Condition 2: O- Medical and Surgical

• Registration Number: CTRI/2023/10/058741
• Lead Sponsor: Rabindranath Tagore Medical College

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Results First Posted: 1900-01-01
• Last Update Posted: 13 November 2023

Recruitment & Eligibility

• Status: ot Yet Recruiting
• Sex: Not specified
• Target Recruitment: 0

Inclusion Criteria

age 18-40 years old, ASA physical status II (uncomplicated pregnancy comes in ASA II), Full term parturients scheduled for elective and semielective LSCS under spinal anaesthesia for indications like previous LSCS, primi breech, postdatism, cord around neck, cephalopelvic disproportion, non progress of labour. Height 150-170 cm, weight 45-90kg.

Exclusion Criteria

Patient refusal.

Patient with contraindication to spinal anaesthesia like coagulopathies or anticoagulant medication, raised intracranial pressure, local puncture site infection etc.

Any cardiac, neurological, renal, liver, endocrine, hematological or any coexisting systemic medical comorbidity, short stature, obesity (BMI more than 30 kg/m2).

Difficult airway, anticipated difficult spinal kyphocoliosis, obese, prior spine surgery.

Emergency LSCS.

Any obstetric comorbidity like antepartum hemorrhage, gestational diabetes etc.

History of allergy to study drugs.

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Duration of sensory blockadeTimepoint: Upto 3 hours postoperatively

Secondary Outcome Measures

Name	Time	Method
Intraoperative hemodynamics & side effects.Timepoint: upto 24 hours postoperatively.